US3919149A - Wax emulsions - Google Patents

Wax emulsions Download PDF

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US3919149A
US3919149A US464717A US46471774A US3919149A US 3919149 A US3919149 A US 3919149A US 464717 A US464717 A US 464717A US 46471774 A US46471774 A US 46471774A US 3919149 A US3919149 A US 3919149A
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emulsion
emulsifier
copolymer
wax
weight
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US464717A
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Donald R Cushman
John W Schick
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ExxonMobil Oil Corp
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Mobil Oil Corp
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    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/60Waxes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • C08L91/06Waxes
    • C08L91/08Mineral waxes
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/34Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/35Polyalkenes, e.g. polystyrene

Definitions

  • This invention relates to wax emulsion compositions and, in one of its aspects, relates more specifically to aqueous wax emulsions particularly suitable for use in internal sizing of photographic paper, and other cellulosic materials, for providing resistance to water, acids, alkali and alcoholic media.
  • photographic paper and other cellulosic materials have been internally sized to provide resistance to water and other liquids such as acids, alkali and alcohols.
  • the most conventionally employed sizing agent comprises sodium stearate, which is precipated by aluminum salts to form aluminum stearate, prior to sheet formation.
  • resistance to acids such as acetic acid, alkali and alcohol has been found to be only fair. and therefore, improvement in such regard is found to be highly desirable.
  • the use of wax emulsions has also been carried out experimentally and, here also, only fair resistance to acid, alkali or alcohol media have been obtained.
  • aqueous wax emulsions can be provided which are suitable for use in internal sizing of photographic paper and other cellulosic materials, by incorporating in the wax emulsions minor amounts of a copolymer of ethylene and acrylic acid.
  • the novel aqueous wax emulsions of the present invention contain a minor amount of a copolymer of ethylene and acrylic acid, a minor amount of an emulsifier and water in an amount sufficient to form the emulsion.
  • the novel aqueous wax emulsion of the present invention for most uses, comprises from about 30% to about 60%, and preferably from about 40% to about 50%, by weight, of a paraffin wax; from about 0.2% to about 10%, and preferably from about 1% to about by weight of a copolymer of ethylene and acrylic acid; from about 2% to about and preferably from about 3% to about 6%, of an emulsifier; and water in an amount sufficient to form the emulsion.
  • the wax component of the emulsion may comprise any paraffin wax obtained from petroleum oil.
  • These waxes may comprise high molecular weight hydrocarbons comprising generally, straight-chain compounds having a crystalline structure in solid form.
  • high molecular weight hydrocarbons comprising generally, straight-chain compounds having a crystalline structure in solid form.
  • the paraffin wax has a melting point from about 120 to about I75F.
  • the copolymer of ethylene and acrylic acid is commercially available.
  • This copolymer has a hardness (ASTM D-S) from about l to about 5', a viscosity-cps 284F. (Brookfield) from about 350 to about 800: and an acid No. from about to about 90.
  • the emulsifier employed in the novel wax emulsion may be of the non-ionic type, anionic type 'or cationic type.
  • the emulsifier may also include emulsifiers of the non-ionic type in combination with the emulsifier of the anionic type. Furthermore. ployed which arecombinations of the non-ionic and cationic types.
  • Many non-ionic emulsifiers can be emernulsifiers may be employed in the emulsion, provided the critical relationship between oil solubility and water solubility is maintained. Typical of such emulsifiers are mixtures of sorbitan monostearate and polyoxyethylene sorbitan monooleate.
  • non-ionic emulsifiers suitable for use in the wax emulsion are polyoxyethylene ethers and octyl or nonyl phenol having variable amounts of ethylene oxide content per mole of finished product required to provide oil and water solubility characteristics.
  • Emulsifiers of the anionic type may include soaps of fatty acids and alkanolamines.
  • such anb nic emulsifiers as lignin sulfonates, naphthalene sulfonates and protective colloids such as natural gums; gelatin and the like may also be employed.
  • Particularly preferred are emulsifiers comprising nonionic and anionic type emulsifiers.
  • Representative of the cationic emulsifiers are amine acetates, and in this respect, cationic emulsifiers may also be employed in combination with the aforementioned non-ionic emulsifiers.
  • novel wax emulsions of the present invention may also be employed for such purpose in treating other cellulosic materials such as cotton cloth, cotton tapes. pressboard, wood and similar materials.
  • the wax emulsions may be incorporated in the cellulosic material in any desired amount. In many applications. the emulsions may be employed in such amounts that the emulsion solids imposed on the dry fiber range from about 0.2% to about 5% and, preferably, from about I.()% to about 1.5% of the total weight of the fiber.
  • the Cobb Test serves to measure the resistance of the paper against 60%, by weight, of acetic acid.
  • cc of the 60% acetic acid contacts one side of a weighed test sheet (sized in laboratory equipment with 1.5%, by weight, solids of the experimental sizing agent) for a period of 60 seconds.
  • the acid is then poured off, excess acid is blotted off, and the sheet reweighed to determine the weight of acetic acid retained. This weight is multiplied by a factor to show grams of acid retained per square meter surface area of paper contacted.
  • copolymer l (ethylene/acrylic acid) had a softening point (ASTM E-28) of 2l5F.; a hardness dmm (ASTM D-S) of 4.0; a density g/cc (ASTM D- l505) of 0.93; a viscosity-cps 284F. (Brookfield) of 650; and an acid no. of 75.
  • Polymer (2) comprised oxidized polyethylene having a sofiening point (ASTM 5-28) of 219F. a hardness (ASTM D-S) of 5.5; a density g/cc (ASTM D1505) of 0.93; viscosity-cps 284F.
  • Polymer (3) comprised oxidized polyethylene having a softening point (ASTM 5-28) of 205F.', a hardness (ASTM D-5) of 12; a density g/cc (ASTM D1505) of 0.92; viscosity-cps 284F. (Brookfield) of I20; and an acid no. of 15.
  • Polymer (4) comprised oxidized polyethylene hav- Table l SIZING AGENTS AND PERFORMANCE Ex. I Ii ⁇ . 2 Ex. 3 Ex. 4 Ev 5 133/135 A. ⁇ IP Refined Paraffin (in 4
  • Table II the results ob tained employing higher melting waxes, in which the resistance of the paper against 60%, by weight. of acetic acid are measured by the Cobb Test. as in Table I.
  • Table II the same copolymer of ethylene and acrylic acid was employed as well as the same non-ionic and anionic emulsifiers of Table I. All parts of the components of Table II, as in Table I. are expressed in weight percent.
  • the wax emulsion containing the aforementioned ethylene/acrylic copolymer exhibited a performance value of 14.6, contrasted with poor performance values when the copolymer was omitted from the wax emulsion. It will also be noted from Table 11 that sodium stearate. as a sizing agent. had the least resistance to acetic acid.
  • aqueous wax emulsions can be prepared which are suitable for use in internal sizing of photographic paper and other cellulosic materials by incorporating in the wax emulsion minor amounts of a copolymer of ethylene acrylic acid.
  • aqueous wax emulsion containing from about 30% to about 60%. by weight. paraffin wax: from about 0.2% to 10% of a copolymer of ethylene and acrylic acid having a hardness (ASTM D-S) from about 1 to about 5. a viscosity cps. (Brookfield) from about 350 to about 800. and an acid No. from about 30 to about 90; a minor amount of an emulsifier; and water in an amount sufficient to form the emulsion.
  • emulsion of claim 1 wherein said emulsion comprises, by weight. from about 2% to about emulsifier. and water in an amount sufficient to form the emulsion.
  • the emulsion of claim 1 wherein said emulsion comprises, by weight. from about to about paraffin wax. from about l% to about 5% of the copolymer of ethylene and acrylic acid, from about 3% to about 67: emulsifier and water in an amount sufficient to form the emulsion.
  • paraffin wax has a melting point from about 120F. to about 175F.

Abstract

Aqueous wax emulsions containing a minor amount of a copolymer of ethylene and acrylic acid, a minor amount of an emulsifier, and water in an amount sufficient to form the emulsion.

Description

United States Patent 11 1 Cushman et a1.
[5 WAX EMULSIONS 175] Inventors: Donald R. Cushman, Wenonah;
John W. Schick, Cherry H111, both of 21 Appl. No: 464,717
[52] US. Cl ,4 260/285 AV: 1 17/155 UA;
260/285 R [51] Int. C15 a COSL 91/00 [58] Field 01" Search H 260/285 R. 285 AV;
1451 Nov. 11, 1975 [56] References Cited UNITED STATES PATENTS 3.741.935 6/1973 McDonald 20012525 R 3.756973 9/1973 Stah1.............. 160/185 R Primary E,\'umiue1'Me1vyn 1. Marquis Almmey, Agent or Finn-Charles A. Huggctt; Raymond W. Barclay; Benjamin 1. Kaufman [57] ABSTRACT Aqueous wax emulsions containing a minor amount 01 a copolymer of ethylene and acrylic acid. a minor amount of an emulsifien and water in an amount sufficient to form the emulsion 8 Claims. N0 Drawings wxx EMULSIONS BACKGROUND OF THE INVENTION 1. Field of the Invention This invention relates to wax emulsion compositions and, in one of its aspects, relates more specifically to aqueous wax emulsions particularly suitable for use in internal sizing of photographic paper, and other cellulosic materials, for providing resistance to water, acids, alkali and alcoholic media.
2. Description of the Prior Art Prior to the present invention, photographic paper and other cellulosic materials, have been internally sized to provide resistance to water and other liquids such as acids, alkali and alcohols. The most conventionally employed sizing agent comprises sodium stearate, which is precipated by aluminum salts to form aluminum stearate, prior to sheet formation. Although good water resistance has been obtained by such procedure, resistance to acids such as acetic acid, alkali and alcohol has been found to be only fair. and therefore, improvement in such regard is found to be highly desirable. The use of wax emulsions has also been carried out experimentally and, here also, only fair resistance to acid, alkali or alcohol media have been obtained.
SUMMARY OF THE INVENTION It has now been found that aqueous wax emulsions can be provided which are suitable for use in internal sizing of photographic paper and other cellulosic materials, by incorporating in the wax emulsions minor amounts of a copolymer of ethylene and acrylic acid. in general, as more fully hereinafter described, the novel aqueous wax emulsions of the present invention contain a minor amount of a copolymer of ethylene and acrylic acid, a minor amount of an emulsifier and water in an amount sufficient to form the emulsion.
In its more specific aspects, the novel aqueous wax emulsion of the present invention, for most uses, comprises from about 30% to about 60%, and preferably from about 40% to about 50%, by weight, of a paraffin wax; from about 0.2% to about 10%, and preferably from about 1% to about by weight of a copolymer of ethylene and acrylic acid; from about 2% to about and preferably from about 3% to about 6%, of an emulsifier; and water in an amount sufficient to form the emulsion.
The wax component of the emulsion may comprise any paraffin wax obtained from petroleum oil. These waxes may comprise high molecular weight hydrocarbons comprising generally, straight-chain compounds having a crystalline structure in solid form. Preferably,
the paraffin wax has a melting point from about 120 to about I75F.
The copolymer of ethylene and acrylic acid is comercially available. This copolymer has a hardness (ASTM D-S) from about l to about 5', a viscosity-cps 284F. (Brookfield) from about 350 to about 800: and an acid No. from about to about 90.
The emulsifier employed in the novel wax emulsion may be of the non-ionic type, anionic type 'or cationic type. The emulsifier may also include emulsifiers of the non-ionic type in combination with the emulsifier of the anionic type. Furthermore. ployed which arecombinations of the non-ionic and cationic types. Many non-ionic emulsifiers can be emernulsifiers may be employed in the emulsion, provided the critical relationship between oil solubility and water solubility is maintained. Typical of such emulsifiers are mixtures of sorbitan monostearate and polyoxyethylene sorbitan monooleate. Typical other non-ionic emulsifiers suitable for use in the wax emulsion are polyoxyethylene ethers and octyl or nonyl phenol having variable amounts of ethylene oxide content per mole of finished product required to provide oil and water solubility characteristics. Emulsifiers of the anionic type may include soaps of fatty acids and alkanolamines. In addition, such anb nic emulsifiers as lignin sulfonates, naphthalene sulfonates and protective colloids such as natural gums; gelatin and the like may also be employed. Particularly preferred are emulsifiers comprising nonionic and anionic type emulsifiers. Representative of the cationic emulsifiers are amine acetates, and in this respect, cationic emulsifiers may also be employed in combination with the aforementioned non-ionic emulsifiers.
The novel wax emulsions of the present invention, although particularly advantageously employed in the internal sizing of photographic papers to make them resistant to water, acid, alkali and alcoholic media, may also be employed for such purpose in treating other cellulosic materials such as cotton cloth, cotton tapes. pressboard, wood and similar materials. The wax emulsions may be incorporated in the cellulosic material in any desired amount. In many applications. the emulsions may be employed in such amounts that the emulsion solids imposed on the dry fiber range from about 0.2% to about 5% and, preferably, from about I.()% to about 1.5% of the total weight of the fiber.
DESCRIPTION OF SPECIFIC EMBODIMENTS The following comparative data and examples will serve to illustrate the effect of the novel wax emulsions of the present invention as internal sizing agents for cellulosic materials. The following Table l is intended to illustrate the use of both copolymers of ethylene and acrylic acid and also polymeric materials as internal sizing agents for paper and respective performance data obtained, as measured by the Cobb Test.
The Cobb Test serves to measure the resistance of the paper against 60%, by weight, of acetic acid. In this test, cc of the 60% acetic acid contacts one side of a weighed test sheet (sized in laboratory equipment with 1.5%, by weight, solids of the experimental sizing agent) for a period of 60 seconds. The acid is then poured off, excess acid is blotted off, and the sheet reweighed to determine the weight of acetic acid retained. This weight is multiplied by a factor to show grams of acid retained per square meter surface area of paper contacted.
In Table I, copolymer l (ethylene/acrylic acid) had a softening point (ASTM E-28) of 2l5F.; a hardness dmm (ASTM D-S) of 4.0; a density g/cc (ASTM D- l505) of 0.93; a viscosity-cps 284F. (Brookfield) of 650; and an acid no. of 75. Polymer (2) comprised oxidized polyethylene having a sofiening point (ASTM 5-28) of 219F. a hardness (ASTM D-S) of 5.5; a density g/cc (ASTM D1505) of 0.93; viscosity-cps 284F. (Brookfield) of 200; and an acid no. of IS. Polymer (3) comprised oxidized polyethylene having a softening point (ASTM 5-28) of 205F.', a hardness (ASTM D-5) of 12; a density g/cc (ASTM D1505) of 0.92; viscosity-cps 284F. (Brookfield) of I20; and an acid no. of 15. Polymer (4) comprised oxidized polyethylene hav- Table l SIZING AGENTS AND PERFORMANCE Ex. I Ii\. 2 Ex. 3 Ex. 4 Ev 5 133/135 A.\IP Refined Paraffin (in 4|.ll -ll.Il 41.11 41.0 41.0 Micro Crystalline Wm 4.11 3.1! 3.11 3.0 31! ('opoly mer I I 1.0 Polymer (Z1 1.1] Polymer 31 1.0 Polymer 14) 1.0 Non-ionic emulsifier I.h I.h Ln 1.6 1.6 Anionic emulsifier 1.3 1.3 1.3 1.3 1.3 52.1 52.1 531 52.1 52.1
A ater Performance (in paper sized with 1.5, solids from each of alum: t. (obb Testbtli acetic acid grams picked up per sq. meter 45.8 111.1 27.8
IJI
4 In the following Table III is shown a comparison between the effect of employing an emulsion containing copolymers ofethylene and acrylic acid as sizing agents and sodium stearate. as a conventional sizing agent. In obtaining the comparative data of Table III. the Fotosize Test was employed. which comprises an accurate means for measuring penetration into a sized sheet. A mixture of 60%. by weight. of glacial acetic acid and 40%. by weight, of ink is placed in a ring on top of the test sheet which is illuminated from below. Reflectance from below is measured with a photocell, and the time is automatically measured until the ink penetrates the sheet resulting in a reflectance low enough to stop the timer. The time. in seconds, is indicated corresponding to a definite degree of penetration of ink. As shown in Table III. the wax emulsion of Example 3 of Table II. containing the aforementioned ethylene/acrylic acid copolymer in the wax emulsion was greatly superior to sodium stearate as a sizing agent.
Table III COMPARISON OF SIZED PAPER t 1.5%; SIZINGI USING FOTOSIZE TEST FOR ACID RESISTANCE As will be apparent from the foregoing Table l. the wax emulsion containing the aforementioned ethylene/acrylic acid copolymer exhibited a performance value of 18.3 contrasted with poor performance values when oxidized polyethylenes were substituted therefor.
In the following Table II. are shown the results ob tained employing higher melting waxes, in which the resistance of the paper against 60%, by weight. of acetic acid are measured by the Cobb Test. as in Table I. In the examples of Table II, the same copolymer of ethylene and acrylic acid was employed as well as the same non-ionic and anionic emulsifiers of Table I. All parts of the components of Table II, as in Table I. are expressed in weight percent.
Table II SIZING AGENTS AND PERFORMANCE Performance (in paper sized with 1.5) solids from above! Cobb Test. bll'i acetic acid grams picked up/sq. meter 14.6
As will be apparent from the foregoing Table II, the wax emulsion containing the aforementioned ethylene/acrylic copolymer exhibited a performance value of 14.6, contrasted with poor performance values when the copolymer was omitted from the wax emulsion. It will also be noted from Table 11 that sodium stearate. as a sizing agent. had the least resistance to acetic acid.
Table IV EXPERIMENTAL PAPER MACHINE SIZING RESULTS Ex. I of Ex. 2 of E\v 3 of Table II Table II Table II Wax melt pt. F. 143/145 lit! 150 Copolymer *Copolymer l l of Table I1) Fotosize Test. seconds 79 I 28 I 43 "I.l|1 ot'emulsion Paper sized with 15'' sizing solids. time in seconds to penetrate sheet.
As will be noted from the foregoing disclosure and data obtained, aqueous wax emulsions can be prepared which are suitable for use in internal sizing of photographic paper and other cellulosic materials by incorporating in the wax emulsion minor amounts of a copolymer of ethylene acrylic acid. Although the present invention has been described herein by means of certain specific embodiments and illustrative examples, it is not intended that the scope thereof be limited in any way and is capable of various modifications and adaptations as those skilled in the art will readily appreciate.
We claim:
I. An aqueous wax emulsion containing from about 30% to about 60%. by weight. paraffin wax: from about 0.2% to 10% of a copolymer of ethylene and acrylic acid having a hardness (ASTM D-S) from about 1 to about 5. a viscosity cps. (Brookfield) from about 350 to about 800. and an acid No. from about 30 to about 90; a minor amount of an emulsifier; and water in an amount sufficient to form the emulsion.
2. The emulsion of claim 1 wherein said emulsion comprises, by weight. from about 2% to about emulsifier. and water in an amount sufficient to form the emulsion.
3. The emulsion of claim 1 wherein said emulsion comprises, by weight. from about to about paraffin wax. from about l% to about 5% of the copolymer of ethylene and acrylic acid, from about 3% to about 67: emulsifier and water in an amount sufficient to form the emulsion.
4. The emulsion of claim 1 wherein the paraffin wax has a melting point from about 120F. to about 175F.

Claims (8)

1. AN EQUEOUS WAX EMULSION CONTAINING FROM ABOUT 30% TO ABOUT 60%, BY WEIGHT, PARAFFIN WAX FROM ABOUT 0.2% TO 10% OF A COPOLYMER OFF THYLENE AND ACRYLIC ACID HAVING A HARDNESS (ASTM D-5) FROM ABOUT 1 TO ABOUT 5, A VISCOSITY-CPS. (BROOKFIELD) FROM ABOUT 3500 TO ABOUT 80, AND AN ACID NO. FROM ABOUT 30 TO ABOUT 90, A MINOR AMOUNT OF AN EMULSIFER, AND WATER IN AN AMOUNT SUFFICIENT TO FORM THE EMULSION.
2. The emulsion of claim 1 wherein said emulsion comprises, by weight, from about 2% to about 10% emulsifier, and water in an amount sufficient to form the emulsion.
3. The emulsion of claim 1 wherein said emulsion comprises, by weight, from about 40% to about 50% paraffin wax, from about 1% to about 5% of the copolymer of ethylene and acrylic acid, from about 3% to about 6% emulsifier and water in an amount sufficient to form the emulsion.
4. The emulsion of claim 1 wherein the paraffin wax has a melting point from about 120*F. to about 175*F.
5. The emulsion of claim 1 wherein the copolymer has a softening point (ASTM E-28) from about 200*F. to about 250*F.
6. The emulsion of claim 1 wherein the emulsifier is a non-ionic emulsifier comprising a mixture of sorbitan monostearate and polyoxyethylene sorbitan monooleate.
7. The emulsion of claim 1 wherein the emulsifier is an anionic emulsifier comprising a soap obtained by the reaction of a fatty acid and an alkanolamine.
8. The emulsion of claim 1 wherein the emulsifier is a cationic emulsifier comprising an amine acetate.
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Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2540643A1 (en) * 1983-02-04 1984-08-10 Schoeller F Jun Gmbh Co Kg Paper support for photographic layers
US4598019A (en) * 1983-12-06 1986-07-01 Nippon Oil Company, Ltd. Method for surface treatment of powdery and granular material stored in open air
US5539035A (en) * 1994-10-12 1996-07-23 The Mead Corporation Recyclable wax-coated containers
US5624996A (en) * 1987-08-14 1997-04-29 Mitsui Petrochemical Industries, Ltd. Dispersion of fine particles of modified polyethylene and process for preparation thereof
WO1997022754A1 (en) * 1995-12-05 1997-06-26 The Dow Chemical Company Method for externally sizing fibrous materials
WO1998003731A1 (en) * 1996-07-19 1998-01-29 The Dow Chemical Company Internally sized cellulosic products and method for making same
US5756112A (en) * 1995-04-27 1998-05-26 The Procter & Gamble Company Carrier substrate treated with high internal water phase inverse emulsion made with an organopolysiloxane-polyoxyalkylene emulsifier
US5763332A (en) * 1996-04-30 1998-06-09 The Procter & Gamble Company Cleaning articles comprising a polarphobic region and a high internal phase inverse emulsion
US5795932A (en) * 1992-07-08 1998-08-18 Sequa Chemicals, Inc. Surface sizing composition
US5863663A (en) * 1994-11-09 1999-01-26 The Procter & Gamble Company Wet-like cleaning wipes and like articles comprising a carrier treated with an emulsion having a continuous lipid phase
US5908707A (en) * 1996-12-05 1999-06-01 The Procter & Gamble Company Cleaning articles comprising a high internal phase inverse emulsion and a carrier with controlled absorbency
US5939479A (en) * 1991-11-22 1999-08-17 Avery Dennison Corporation Removable and guillotinable emulsion pressure-sensitive adhesives
US5948540A (en) * 1995-04-27 1999-09-07 The Procter & Gamble Company Carrier substrate treated with high internal phase inverse emulsions made with an organopolysiloxane-polyoxyalkylene emulsifier
US5980922A (en) * 1996-04-30 1999-11-09 Procter & Gamble Company Cleaning articles treated with a high internal phase inverse emulsion
US6121165A (en) * 1997-07-31 2000-09-19 The Procter & Gamble Company Wet-like cleaning articles
US6133166A (en) * 1997-07-01 2000-10-17 The Procter & Gamble Company Cleaning articles comprising a cellulosic fibrous structure having discrete basis weight regions treated with a high internal phase inverse emulsion
US20160161696A1 (en) * 2012-10-25 2016-06-09 Commscope Technologies Llc System and method for applying an adhesive coated cable to a surface

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US3741925A (en) * 1971-04-02 1973-06-26 Du Pont Water repellent ethylene copolymer dispersions
US3756973A (en) * 1971-09-20 1973-09-04 Du Pont Dispersion for water repellent coatings

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US3741925A (en) * 1971-04-02 1973-06-26 Du Pont Water repellent ethylene copolymer dispersions
US3756973A (en) * 1971-09-20 1973-09-04 Du Pont Dispersion for water repellent coatings

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2540643A1 (en) * 1983-02-04 1984-08-10 Schoeller F Jun Gmbh Co Kg Paper support for photographic layers
US4598019A (en) * 1983-12-06 1986-07-01 Nippon Oil Company, Ltd. Method for surface treatment of powdery and granular material stored in open air
US5624996A (en) * 1987-08-14 1997-04-29 Mitsui Petrochemical Industries, Ltd. Dispersion of fine particles of modified polyethylene and process for preparation thereof
US5939479A (en) * 1991-11-22 1999-08-17 Avery Dennison Corporation Removable and guillotinable emulsion pressure-sensitive adhesives
US5795932A (en) * 1992-07-08 1998-08-18 Sequa Chemicals, Inc. Surface sizing composition
US5539035A (en) * 1994-10-12 1996-07-23 The Mead Corporation Recyclable wax-coated containers
US5952043A (en) * 1994-11-09 1999-09-14 The Procter & Gamble Company Process for making wet-like cleaning wipes and like articles comprising an emulsion having a continuous lipid phase
US5863663A (en) * 1994-11-09 1999-01-26 The Procter & Gamble Company Wet-like cleaning wipes and like articles comprising a carrier treated with an emulsion having a continuous lipid phase
US5948540A (en) * 1995-04-27 1999-09-07 The Procter & Gamble Company Carrier substrate treated with high internal phase inverse emulsions made with an organopolysiloxane-polyoxyalkylene emulsifier
US5756112A (en) * 1995-04-27 1998-05-26 The Procter & Gamble Company Carrier substrate treated with high internal water phase inverse emulsion made with an organopolysiloxane-polyoxyalkylene emulsifier
US6482886B1 (en) 1995-12-05 2002-11-19 The Dow Chemical Company Method for externally sizing fibrous materials
WO1997022754A1 (en) * 1995-12-05 1997-06-26 The Dow Chemical Company Method for externally sizing fibrous materials
US5993604A (en) * 1995-12-05 1999-11-30 The Dow Chemical Company Internally sized articles and method for making same
US5763332A (en) * 1996-04-30 1998-06-09 The Procter & Gamble Company Cleaning articles comprising a polarphobic region and a high internal phase inverse emulsion
US6001381A (en) * 1996-04-30 1999-12-14 The Procter & Gamble Company Cleaning articles comprising a polarphobic region and a high internal phase inverse emulsion
US5980922A (en) * 1996-04-30 1999-11-09 Procter & Gamble Company Cleaning articles treated with a high internal phase inverse emulsion
WO1998003731A1 (en) * 1996-07-19 1998-01-29 The Dow Chemical Company Internally sized cellulosic products and method for making same
US5908707A (en) * 1996-12-05 1999-06-01 The Procter & Gamble Company Cleaning articles comprising a high internal phase inverse emulsion and a carrier with controlled absorbency
US6133166A (en) * 1997-07-01 2000-10-17 The Procter & Gamble Company Cleaning articles comprising a cellulosic fibrous structure having discrete basis weight regions treated with a high internal phase inverse emulsion
US6121165A (en) * 1997-07-31 2000-09-19 The Procter & Gamble Company Wet-like cleaning articles
US20160161696A1 (en) * 2012-10-25 2016-06-09 Commscope Technologies Llc System and method for applying an adhesive coated cable to a surface

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